• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

DNA 双链断裂作为神经基因组改变、功能和疾病的驱动因素。

DNA double-strand breaks as drivers of neural genomic change, function, and disease.

机构信息

Howard Hughes Medical Institute, Program in Cellular and Molecular Medicine, Boston Children's Hospital, Department of Genetics, and Department of Pediatrics, Harvard Medical School, Boston, MA 02115, United States.

Department of Neurological Surgery and Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, CA 94158, United States.

出版信息

DNA Repair (Amst). 2018 Nov;71:158-163. doi: 10.1016/j.dnarep.2018.08.019. Epub 2018 Aug 23.

DOI:10.1016/j.dnarep.2018.08.019
PMID:30195640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6340756/
Abstract

Early work from about two decades ago implicated DNA double-strand break (DSB) formation and repair in neuronal development. Findings emerging from recent studies of DSBs in proliferating neural progenitors and in mature, non-dividing neurons suggest important roles of DSBs in brain physiology, aging, cancer, psychiatric and neurodegenerative disorders. We provide an overview of some findings and speculate on what may lie ahead.

摘要

早期约二十年前的工作表明,DNA 双链断裂(DSB)的形成和修复与神经元发育有关。最近对增殖中的神经祖细胞和成熟的、非分裂神经元中的 DSB 的研究结果表明,DSB 在大脑生理学、衰老、癌症、精神疾病和神经退行性疾病中具有重要作用。我们提供了一些研究结果的概述,并对未来可能的发展进行了推测。

相似文献

1
DNA double-strand breaks as drivers of neural genomic change, function, and disease.DNA 双链断裂作为神经基因组改变、功能和疾病的驱动因素。
DNA Repair (Amst). 2018 Nov;71:158-163. doi: 10.1016/j.dnarep.2018.08.019. Epub 2018 Aug 23.
2
Genome Stability by DNA Polymerase β in Neural Progenitors Contributes to Neuronal Differentiation in Cortical Development.神经祖细胞中DNA聚合酶β介导的基因组稳定性对皮质发育中神经元分化的作用
J Neurosci. 2017 Aug 30;37(35):8444-8458. doi: 10.1523/JNEUROSCI.0665-17.2017. Epub 2017 Aug 1.
3
Genomic rearrangements induced by unscheduled DNA double strand breaks in somatic mammalian cells.体细胞哺乳动物细胞中未计划的 DNA 双链断裂诱导的基因组重排。
FEBS J. 2017 Aug;284(15):2324-2344. doi: 10.1111/febs.14053. Epub 2017 Mar 22.
4
Three classes of recurrent DNA break clusters in brain progenitors identified by 3D proximity-based break joining assay.通过基于 3D 邻近的断裂连接分析鉴定的脑祖细胞中三类反复出现的 DNA 断裂簇。
Proc Natl Acad Sci U S A. 2018 Feb 20;115(8):1919-1924. doi: 10.1073/pnas.1719907115. Epub 2018 Feb 5.
5
Transcription-associated DNA DSBs activate p53 during hiPSC-based neurogenesis.转录相关的 DNA DSBs 在基于 hiPSC 的神经发生过程中激活 p53。
Sci Rep. 2022 Jul 15;12(1):12156. doi: 10.1038/s41598-022-16516-5.
6
Imaging Flow Cytometry Quantifies Neural Genome Dynamics.成像流式细胞术定量分析神经基因组动力学。
Cytometry A. 2019 Aug;95(8):825-835. doi: 10.1002/cyto.a.23783. Epub 2019 May 7.
7
Repair kinetics of DNA double-strand breaks and incidence of apoptosis in mouse neural stem/progenitor cells and their differentiated neurons exposed to ionizing radiation.暴露于电离辐射下的小鼠神经干/祖细胞及其分化神经元中DNA双链断裂的修复动力学和细胞凋亡发生率
J Radiat Res. 2018 May 1;59(3):261-271. doi: 10.1093/jrr/rrx089.
8
Long Neural Genes Harbor Recurrent DNA Break Clusters in Neural Stem/Progenitor Cells.长神经基因在神经干/祖细胞中存在反复出现的DNA断裂簇。
Cell. 2016 Feb 11;164(4):644-55. doi: 10.1016/j.cell.2015.12.039.
9
Repair Pathway Choices and Consequences at the Double-Strand Break.双链断裂处的修复途径选择及其后果
Trends Cell Biol. 2016 Jan;26(1):52-64. doi: 10.1016/j.tcb.2015.07.009. Epub 2015 Oct 1.
10
[The main repair pathways of double-strand breaks in the genomic DNA and interactions between them].[基因组DNA中双链断裂的主要修复途径及其相互作用]
Tsitol Genet. 2014 May-Jun;48(3):64-77.

引用本文的文献

1
Crosstalk between DNA damage and cGAS-STING immune pathway drives neuroinflammation and dopaminergic neurodegeneration in Parkinson's disease.DNA损伤与cGAS-STING免疫通路之间的串扰驱动帕金森病中的神经炎症和多巴胺能神经变性。
Brain Behav Immun. 2025 Jul 31:106065. doi: 10.1016/j.bbi.2025.106065.
2
Double strand breaks drive toxicity in Huntington's disease mice with or without somatic expansion.双链断裂在有或没有体细胞扩增的亨廷顿舞蹈症小鼠中引发毒性。
bioRxiv. 2025 May 28:2025.05.27.654663. doi: 10.1101/2025.05.27.654663.
3
Analysis of rad-51 separation of function allele suggests divergence of the synthesis-dependent strand annealing and double Holliday junction pathways prior to RAD-51 filament disassembly.

本文引用的文献

1
Three classes of recurrent DNA break clusters in brain progenitors identified by 3D proximity-based break joining assay.通过基于 3D 邻近的断裂连接分析鉴定的脑祖细胞中三类反复出现的 DNA 断裂簇。
Proc Natl Acad Sci U S A. 2018 Feb 20;115(8):1919-1924. doi: 10.1073/pnas.1719907115. Epub 2018 Feb 5.
2
DNA double-strand break response factors influence end-joining features of IgH class switch and general translocation junctions.DNA 双链断裂反应因子影响 IgH 类别转换和一般易位连接点的连接特征。
Proc Natl Acad Sci U S A. 2018 Jan 23;115(4):762-767. doi: 10.1073/pnas.1719988115. Epub 2018 Jan 8.
3
Synaptic Neurexin Complexes: A Molecular Code for the Logic of Neural Circuits.
对功能等位基因的rad-51分离分析表明,在RAD-51细丝解体之前,合成依赖链退火和双Holliday连接途径就已出现分歧。
Genetics. 2025 Jun 4;230(2). doi: 10.1093/genetics/iyaf063.
4
XRCC4-related microcephalic primordial dwarfism: description of a clinical series of 7 cases, phenotype expansion and new diagnostic approaches.与XRCC4相关的小头畸形原发性侏儒症:7例临床系列描述、表型扩展及新的诊断方法
Eur J Hum Genet. 2025 Mar 20. doi: 10.1038/s41431-025-01821-0.
5
Proteins Associated with Neurodegenerative Diseases: Link to DNA Repair.与神经退行性疾病相关的蛋白质:与DNA修复的联系
Biomedicines. 2024 Dec 11;12(12):2808. doi: 10.3390/biomedicines12122808.
6
CRISPR/Cas9-induced double-strand breaks in the huntingtin locus lead to CAG repeat contraction through DNA end resection and homology-mediated repair.CRISPR/Cas9诱导的亨廷顿蛋白基因座双链断裂通过DNA末端切除和同源介导的修复导致CAG重复序列收缩。
BMC Biol. 2024 Dec 3;22(1):282. doi: 10.1186/s12915-024-02079-6.
7
Base excision repair and double strand break repair cooperate to modulate the formation of unrepaired double strand breaks in mouse brain.碱基切除修复和双链断裂修复合作调节小鼠大脑中未修复双链断裂的形成。
Nat Commun. 2024 Sep 4;15(1):7726. doi: 10.1038/s41467-024-51906-5.
8
Early oxidative stress and DNA damage in Aβ-burdened hippocampal neurons in an Alzheimer's-like transgenic rat model.阿尔茨海默病样转基因大鼠模型中海马神经元中 Aβ 负荷引起的早期氧化应激和 DNA 损伤。
Commun Biol. 2024 Jul 14;7(1):861. doi: 10.1038/s42003-024-06552-4.
9
Neuronal DNA repair reveals strategies to influence CRISPR editing outcomes.神经元DNA修复揭示了影响CRISPR编辑结果的策略。
bioRxiv. 2025 Mar 17:2024.06.25.600517. doi: 10.1101/2024.06.25.600517.
10
A Unifying Hypothesis for the Genome Dynamics Proposed to Underlie Neuropsychiatric Phenotypes.一个被认为是神经精神疾病表型基础的基因组动力学统一假说。
Genes (Basel). 2024 Apr 8;15(4):471. doi: 10.3390/genes15040471.
突触神经连接蛋白复合体:神经回路逻辑的分子编码
Cell. 2017 Nov 2;171(4):745-769. doi: 10.1016/j.cell.2017.10.024.
4
Genome integrity and disease prevention in the nervous system.神经系统中的基因组完整性与疾病预防
Genes Dev. 2017 Jun 15;31(12):1180-1194. doi: 10.1101/gad.301325.117.
5
Genome Organization Drives Chromosome Fragility.基因组组织驱动染色体脆弱性。
Cell. 2017 Jul 27;170(3):507-521.e18. doi: 10.1016/j.cell.2017.06.034. Epub 2017 Jul 20.
6
Physiological functions of programmed DNA breaks in signal-induced transcription.信号诱导转录中程序性DNA断裂的生理功能。
Nat Rev Mol Cell Biol. 2017 Aug;18(8):471-476. doi: 10.1038/nrm.2017.43. Epub 2017 May 24.
7
Non-homologous DNA end joining and alternative pathways to double-strand break repair.非同源DNA末端连接及双链断裂修复的替代途径。
Nat Rev Mol Cell Biol. 2017 Aug;18(8):495-506. doi: 10.1038/nrm.2017.48. Epub 2017 May 17.
8
Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network.不同神经元基因组与神经精神疾病的交叉点:大脑体细胞镶嵌网络。
Science. 2017 Apr 28;356(6336). doi: 10.1126/science.aal1641. Epub 2017 Apr 27.
9
The Role of Epigenetic Mechanisms in the Regulation of Gene Expression in the Nervous System.表观遗传机制在神经系统基因表达调控中的作用
J Neurosci. 2016 Nov 9;36(45):11427-11434. doi: 10.1523/JNEUROSCI.2492-16.2016.
10
Topoisomerase II beta interacts with cohesin and CTCF at topological domain borders.拓扑异构酶IIβ在拓扑结构域边界与黏连蛋白和CTCF相互作用。
Genome Biol. 2016 Aug 31;17(1):182. doi: 10.1186/s13059-016-1043-8.